US5840692A

US5840692A - Peptide fragments and analogs of thrombospondin

Info

Publication number: US5840692A
Application number: US08/488,273
Authority: US
Inventors: Alan Howard Deutch; George Paul Tuszynski
Original assignee: WR Grace and Co Conn; Drexel University College of Medicine
Current assignee: WR Grace and Co Conn; Drexel University College of Medicine
Priority date: 1990-02-22
Filing date: 1995-06-07
Publication date: 1998-11-24
Anticipated expiration: 2015-11-24

Abstract

Compounds and compositions comprising fragments and synthetic analogs of human thrombospondin are provided together with methods for their use as thrombospondin-like agents.

Description

This application is a continuation-in-part application of application Ser. No. 359,263 filed Dec. 19, 1994, now abandoned which is in turn a divisional application of application Ser. No. 110,146 filed Aug. 20, 1993, now issued U.S. Pat. No. 5,426,100 (issued Jun. 20, 1995), which is in turn a continuation of application Ser. No. 896,527 filed Jun. 9, 1992, now abandoned, and which is in turn a divisional application of application Ser. No. 483,527 filed Feb. 22, 1990, now issued U.S. Pat. No. 5,190,918 (issued Mar. 2, 1993 ).

TECHNICAL FIELD

The present invention relates generally to peptide fragments and synthetic analogs of thrombospondin which retain thrombospondin-like activity. The peptides find use as agents in anti-tumor development, wound healing, atherosclerosis, antimalaria, antithrombotics, thrombolytics, angiogenesis, complement activation, cell attachment, diagnostic reagents and other related areas.

BACKGROUND

Thrombospondin (also known as thrombin sensitive protein or TSP) is a large molecular weight 180 kD glycoprotein composed of three identical disulfide-linked polypeptide chains. Thrombospondin has been purified by a number or procedures including exclusion chromatography (Lawler et al., J. Biol. Chem. (1978) 253:8609-16), heparin affinity chromatography (Lawler et al., Thromb. Res. (1981) 22:267-269), fibrinogen affinity chromatography (Tuszynski et al., J. Biol. Chem. (1985) 260:12240-5), barium chloride precipitation (Alexander et al., Biochem. J. (1984) 217:67-71) and anion exchange chromatography with HPLC (Clezarolin et al., J. Chromatog. (1984) 296:249-56).

The complete amino acid sequence of TSP has been deduced from DNA clones prepared by various groups including Lawler et al., J. Cell Biol. (1986) 103:1635-48; Kobayashi et al., Biochemistry (1986) 25:8418-25; Dixit et al., Proc. Ntl. Acad. Sci. (1986) 83:5449-53; and Hennessy et al., J. Cell Biol. (1989) 108:729-36.

Kobayashi et al. (supra), Robson et al. (Nature (1988) 335:79-82) and Goundis et al. (Nature (1988) 335:82-85) compared the sequences of thrombospondin, thrombospondin-related anonymous protein, properdin, the terminal complement components, and circumsporozoite proteins and recognized a significant homology based around the consensus sequence W-S-P-C-S-V-T-C-G SEQ ID NO:1!. While the sequence homology was recognized, there was no known use for such sequence.

The present invention provides thrombospondin fragments and analogs which mimic or inhibit the biological activity of intact thrombospondin which find use in a variety of biological, prophylactic or therapeutic areas.

SUMMARY OF THE INVENTION

It has now been found that a class of fragments or synthetic analogs of thrombospondin have a variety of uses. These peptides are capable of inhibiting tumor metastasis in mammals in vivo. The peptides are also useful in wound healing, atherosclerosis, malaria, thrombotic, and thrombolytic conditions, angiogenesis, and as cell attachment promoters, complement modulators, and diagnostic reagents and in other related areas. Analogs based on the Type I repeat of thrombospondin described by Lawler et al., (Seminars in Thrombosis & Hemostasis (1987) 13:245-254), Robson et al., supra, and Groundis et al., supra, have been shown to have thrombospondin-like activity. Specifically, analogs based around and including at least a portion of the sequence motif of Robson (supra) W-S-P-C-S-V-T-C-G SEQ ID NO:1! have been shown to have thrombospondin-like activity.

The present invention is, therefore, in one aspect directed to polypeptide compounds having thrombospondin-like activity which are identified by the formula:

Z.sub.1 -AA.sub.1 -AA.sub.2 -AA.sub.3 -AA.sub.4 -AA.sub.5 -AA.sub.6 -AA.sub.7 -AA.sub.8 -AA.sub.9 -Z.sub.2                     SEQ ID NO: 15!

wherein:

AA₁ is a neutral/non-polar/large/cyclic amino acid residue;

AA₂ is a neutral/polar/small or neutral/polar/large/non-cyclic or acidic amino acid residue;

AA₃ is a neutral/nonpolar/large/cyclic or neutral/non-polar/large/non-cyclic or neutral/polar/large/non-cyclic or neutral/polar/small amino acid residue;

AA₄ is a neutral/polar/small amino acid residue;

AA₅ is a neutral/polar/small or neutral/polar/large/non-cyclic amino acid residue;

AA₆ is a neutral/nonpolar/large/non-cyclic or neutral/polar/large/non-cyclic amino acid residue;

AA₇ is a neutral/polar/large/non-cyclic or neutral/polar/small amino acid residue;

AA₈ is a neutral/polar/small amino acid residue;

AA₉ is a neutral/polar/small amino acid residue;

Z₁ is hydrogen, amino, acetyl or at least one amino acid residue or the desamino form thereof;

Z₂ is hydroxyl, carboxyl, non-amino acids such as agmatine, or at least one amino acid residue, including carboxyamide or alkylamide forms thereof.

Also provided in accordance with aspects of the invention are pharmaceutical compositions which contain the above-recited polypeptide compounds together with a pharmaceutically acceptable liquid, gel or solid carrier. Administration of therapeutically effective doses of these compositions can provide effective enhancement or inhibition of thrombospondin-like activity to animals, particularly vertebrates such as mammalian and avian hosts.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts the in vitro ability of selected peptide compounds of the present invention to inhibit platelet aggregation.

DETAILED DESCRIPTION OF THE INVENTION

In accordance with the present invention, a class of fragments and analogs of thrombospondin is provided which is capable of inhibiting or mimicing the activity of thrombospondin in mammals in vivo.

A. Definitions

"Thrombospondin-like activity" is defined herein as any activity that mimics the known biological activities of thrombospondin. These activities include cell-adhesion promoting activity, cell mitogenic activity, cell chemotactic activities, and hemostatic activities and any activities that derive from these activities such as tumor cell, microbial, or parasite metastasis activity, platelet aggregating activity, fibrinolytic activity and immune modulation.

"Antimetastatic activity" is defined herein as the ability to prevent or greatly reduce the extent or size of tumor cell metastasis, or inhibit or cause regression of primary solid tumors.

"Wound healing activity" is defined herein as the ability to increase the rate at which wounds heal or to improve the results of the healing process (i.e., less scarring, good response to tactile stimulus, etc.)

"Atherosclerosis activity" is defined herein as the capacity of thrombospondin to either promote or inhibit atherosclerotic lesion formation. The atherosclerotic lesion is defined as the degenerative accumulation of lipid-containing materials, especially in arterial walls.

"Antimalaria activity" is defined herein as the ability to inhibit either the cytoadherence of malarial-infected red blood cells to endothelial cells, the malarial sporozoite recognition and entry into hepatocytes, or the malarial merozoite recognition and entry into red blood cells. Antimalarial activity can be demonstrated in the form of a vaccine or a therapeutic that blocks cytoadherence.

"Antithrombotic activity" is defined herein as the ability to either inhibit the aggregation of platelets or to antagonize the formation of a thrombus.

"Thrombolytic activity" is defined herein as the ability to disrupt the structure of a thrombus.

"Angiogenesis activity" is defined herein as the ability to inhibit or enhance the formation of blood vessels or lymph vessels.

"Growth factor activity" is defined herein as the ability to inhibit or promote cell proliferation.

"Cell adhesion activity" is defined herein as the ability to promote or inhibit the attachment of cells, preferably mammalian cells, to a substrate.

"Complement activity" is defined herein as the ability to activate or block the Complement Cascade Pathway of the immune system.

"Antiviral activity" is defined herein as the ability to prevent or inhibit viral infection by interfering with the ability of the viral particle to bind to cells.

The sequence of amino acid residues of the present polypeptide compounds, the core nonapeptide, and preferred embodiments thereof, are defined in terms of amino acids of certain characteristics of particular subclasses.

Amino acid residues can be generally subclassified into four major subclasses as follows:

Acidic, i.e., the residue has a negative charge due to loss of H ion at physiological pH and the residue is attracted by aqueous solution so as to seek the surface positions in the conformation of a peptide in which it is contained when the peptide is in aqueous medium.

Basic, i.e., the residue has a positive charge due to association with H ion at physiological pH and the residue is attracted by aqueous solution so as to seek the surface positions in the conformation of a peptide in which it is contained when the peptide is in aqueous medium.

Neutral/non-polar, i.e., the residues are not charged at physiological pH and the residue is repelled by aqueous solution so as to seek the inner positions in the conformation of a peptide in which it is contained when the peptide is in aqueous medium.

Neutral/polar, i.e., the residues are not charged at physiological pH and the residue is attracted by aqueous solution so as to seek the outer positions in the conformation of a peptide in which it is contained when the peptide is in aqueous medium.

It is understood, of course, that in a statistical collection of individual residue molecules some molecules will be charged, and some not. To fit the definition of charged, a significant percentage (at least approximately 25%) of the individual molecules are charged at physiological pH.

Amino acid residues can be further subclassified as cyclic or non-cyclic, a self-explanatory classification with respect to the side chain substituent groups of the residues, and as small or large. The residue is considered small if it contains a total of three carbon atoms or less. Small residues are, of course, always non-cyclic.

For the naturally occurring protein amino acids, subclassification according to the foregoing scheme is as follows:

Acidic: Aspartic acid and Glutamic acid;

Basic/non-cyclic: Arginine and Lysine;

Basic/cyclic: Histidine;

Neutral/polar/small: Glycine, Serine and Cysteine;

Neutral/polar/large/non-cyclic: Threonine, Asparagine and Glutamine;

Neutral/polar/large/cyclic: Tyrosine;

Neutral/non-polar/small: Alanine;

Neutral/non-polar/large/non-cyclic: Valine, Isoleucine, Leucine and Methionine;

Neutral/non-polar/large/cyclic: Phenylalanine and Tryptophan.

The protein amino acid proline, although within the classification neutral/non-polar/large/cyclic, is not included as an alternative due to its known effects on the secondary conformation of peptide chains.

Certain commonly encountered non-natural amino acids, such as desamino Tyrosine (des Tyr), agmatine (Agm), n-formyl tryptophan (f-Trp), alpha-aminoisobutyric acid (Aib), and sarcosine (Sar), statine, ornithine (Orn), homolysine, homoserine, homoarginine, norleucine (Nle), norvaline may also be incorporated into the compounds of the invention. Desamino tyrosine is incorporated at the N-terminus. Agmatine and statine are incorporated at the C-terminus. Based on the above definition, n-formyl Trp is neutral/non-polar/large/cyclic, Sar is neutral/non-polar/small, Aib is neutral/non-polar/non-cyclic, Orn is basic/non-cyclic, homolysine is basic/non-cyclic, homoserine is neutral/polar/small, homoarginine is basic/non-cyclic, norleucine is neutral/non-polar/large/non-cyclic, and norvaline is neutral/non-polar/large/non-cyclic.

The nomenclature used to describe polypeptide compounds of the present invention follows the conventional practice wherein the amino group is presented to the left and the carboxy group to the right of each amino acid residue. In the formulae representing selected specific embodiments of the present invention, the amino- and carboxy-terminal groups, although not specifically shown, will be understood to be in the form they would assume at physiologic pH values, unless otherwise specified. In the amino acid structure formulae, each residue is generally represented by a single letter designation, corresponding to the trivial name of the amino acid, in accordance with the following schedule:

______________________________________                                    
               One-letter                                                 
Amino Acid     Symbol                                                     
______________________________________                                    
Alanine        A                                                          
Arginine       R                                                          
Asparagine     N                                                          
Aspartic acid  D                                                          
Cysteine       C                                                          
Glutamine      Q                                                          
Glutamic acid  E                                                          
Glycine        G                                                          
Histidine      H                                                          
Isoleucine     I                                                          
Leucine        L                                                          
Lysine         K                                                          
Methionine     M                                                          
Phenylalanine  F                                                          
Proline        P                                                          
Serine         S                                                          
Threonine      T                                                          
Tryptophan     W                                                          
Tyrosine       Y                                                          
Valine         V                                                          
______________________________________

In the present application, the L-form of any amino acid residue having an optical isomer is intended unless otherwise expressly indicated, e.g., by the symbol " D-AA_n !."

Compounds within the scope of the present invention can be obtained by modifying the disclosed formulae in numerous ways, while preserving the activity of the polypeptide compounds thus obtained. For example, while the amino acids of these compounds are normally in the natural L optical isomer form, one or more, usually two or less and preferably one amino acid may be replaced with the optical isomer D form, or a D,L-racemic mixture can be provided in the molecules comprising the polypeptide compound. Additionally, a disulfide linkage may be present or absent in the compounds of the invention, as long as activity is maintained.

Amino acid residues contained within the compounds, and particularly at the carboxy- or amino-terminus, can also be modified by methylation, amidation, acetylation or substitution with other chemical groups which can, for example, change the circulating half-life, resistance to proteases and solubility of the compounds without adversely effecting their activity.

In addition to the preceding definitions, the following abbreviations have been used throughout in describing the invention:

______________________________________                                    
BCA              bicinchoninic acid                                       
BSA              bovine serum albumin                                     
t-Boc            t-butyloxycarbonyl                                       
Bzl              benzyl                                                   
°C.       degrees centigrade                                       
DCM              dichloromethane                                          
DIEA             diisopropyl ethyl amine                                  
DMEM             Dulbecco's minimum                                       
                 essential medium                                         
DMF              dimethyl formamide                                       
HF               hydrogen fluoride                                        
HOBT             1-hydroxybenzotriazole                                   
HPLC             high performance liquid                                  
                 chromatography                                           
mBHA             methylbenzhydrylamine                                    
μg            microgram                                                
μl            microliter                                               
ml               milliliter                                               
mM               millimolar                                               
nm               nanometers                                               
NMP              N-methylpyrrolidone                                      
%                percent                                                  
PAM              phenylacetamidomethyl                                    
PBS              phosphate buffered saline                                
TFA              trifluoroacetic acid                                     
______________________________________

B. Preferred Embodiments The polypeptide compounds of the invention all contain the core nonapeptide sequence:

Z.sub.1 -AA.sub.1 -AA.sub.2 -AA.sub.3 -AA.sub.4 -AA.sub.5 -AA.sub.6 -AA.sub.7 -AA.sub.8 -AA.sub.9 -Z.sub.2                     SEQ ID NO: 15!

wherein:

AA₁ is a neutral/nonpolar/large/cyclic amino acid residue;

AA₃ is a neutral/nonpolar/large/cyclic or neutral/nonpolar/large/non-cyclic or neutral/polar/large/non-cyclic or neutral/polar/small amino acid residue;

AA₄ is a neutral/polar/small amino acid residue;

AA₆ is a neutral/nonpolar/large/non-cyclic neutral/polar/large/non-cyclic amino acid residue;

AA₈ is a neutral/polar/small amino acid residue

AA₉ is a neutral/polar/small amino acid residue;

Z₁ is hydrogen, amino, acetyl or at least one amino acid residue or the desamino form thereof; and

The most preferred sequence of this core nonapeptide is W-S-P-C-S-V-T-C-G SEQ ID NO:1!. Other preferred embodiments include polypeptide compounds wherein:

______________________________________                                    
AA.sub.1     is tryptophan or n-formyl-tryptophan;                        
AA.sub.2     is serine, threonine or aspartic acid;                       
AA.sub.3     is proline, glutamic acid, serine or                         
             isoleucine;                                                  
AA.sub.4     is cysteine;                                                 
AA.sub.5     is serine or asparagine;                                     
AA.sub.6     is valine or threonine;                                      
AA.sub.7     is threonine or serine;                                      
AA.sub.8     is cysteine;                                                 
AA.sub.9     is glycine or serine, including                              
             carboxyamide forms thereof.                                  
______________________________________

Particularly preferred are those embodiments wherein the sequence is selected from the group consisting of:

__________________________________________________________________________
CompoundStructure                                                         
__________________________________________________________________________
p1WSPCSVTCG                                                               
p5fWSPCSVTCGNH.sub.2  SEQ ID NO:13!                                       
p6WSPCSVTCGNH.sub.2  SEQ ID NO:14!                                        
p18WDICSVTCG  SEQ ID NO:2!                                                
p19WSSCSVTCG  SEQ ID NO:3!                                                
p20WTSCSTSCG  SEQ ID NO:4!                                                
p11WSPWSEWTSCSTSCGNGIQQRGR  SEQ ID NO:5!                                  
p17WSHWSPWSSCSVTCGDGVITRIR  SEQ ID NO:6!                                  
p12WGPWSPWDICSVTCGGGVQKRSR  SEQ ID NO:7!                                  
WSPCSVTCS  SEQ ID NO:8!                                                   
WSQCSVTCG  SEQ ID NO:9!                                                   
WSQCNVTCG  SEQ ID NO:10!                                                  
WTPCSVTCG  SEQ ID NO:11!                                                  
p4DGGWSHWSPWSSCSVTCGDGVITR                                                
IRLCNSPSPQMNGKPCEGEARETKA                                                 
CKKDACPINGG  SEQ ID NO:12!                                                
__________________________________________________________________________

Compounds within the scope of the present invention can be synthesized chemically by means well known in the art such as, e.g., solid phase peptide synthesis. The synthesis is commenced from the carboxy-terminal end of the peptide using an alpha-amino protected amino acid. t-Butylocarbonyl (Boc) protective groups can be used for all amino groups even though other protective groups are suitable. See Stewart et al., "Solid-Phase Peptide Synthesis," W. H. Freeman Co., San Francisco (1969) and Merrifield, J. Am. Chem. Soc. 85: 2149-2154 (1963). These and other methods of peptide synthesis are also exemplified by U.S. Pat. Nos. 3,862,925, 3,842,067, 3,972,859 and 4,105,602.

Conveniently, compounds may be synthesized using manual techniques or automatically employing, for example, an Applied BioSystems 430A Peptide Synthesizer (Foster City, Calif.) or a Biosearch SAM II automatic peptide synthesizer (Biosearch, Inc., San Rafael, Calif.), following the instructions provided in the instruction manual supplied by the manufacturer.

It will be readily appreciated by those having ordinary skill in the art of peptide synthesis that the intermediates which are constructed in accordance with the present disclosure during the course of synthesizing the present compounds are themselves useful compounds and are thus within the scope of the invention.

Alternatively, selected compounds of the present invention can be produced by expression of recombinant DNA constructs prepared in accordance with well-known methods. Such production can be desirable to provide large quantities or alternative embodiments of such compounds.

C. Administration

Compounds of the present invention have thrombospondin-like activity in the intact animal. Compounds of the present invention and compositions containing them which are shown to have the physiological effect of inhibiting or mimicing the effect of intact thrombospondin find use in numerous therapeutic and prophylactic applications, such as cancer therapy, wound healing, atherosclerosis, malaria treatment or prevention, thrombotic or thrombolytic conditions, angiogenesis, complement activation, or cell attachment.

Thus the present invention also provides compositions containing an effective amount of compounds of the present invention, including the nontoxic addition salts, amides and esters thereof, which may, alone, serve to provide the above-recited therapeutic benefits. Such compositions can also be provided together with physiologically tolerable liquid, gel or solid diluents, adjuvants and excipients.

These compounds and compositions can be administered to animals for veterinary use, such as with domestic animals, and clinical use in humans in a manner similar to other therapeutic agents. In general, the dosage required for therapeutic efficacy will range from about 1 μg to 300 mg/kg, more usually 10 μg to 30 mg/kg of the host body weight. Alternatively, dosages within these ranges can be administered by constant infusion over an extended period of time, usually exceeding 24 hours, until the desired therapeutic benefits have been obtained.

Typically, such compositions are prepared as injectables, either as liquid solutions or suspensions; solid forms suitable for solution in, or suspension in, liquid prior to injection may also be prepared. The preparation may also be emulsified. The active ingredient is often mixed with diluents or excipients which are physiologically tolerable and compatible with the active ingredient. Suitable diluents and excipients are, for example, water, saline, dextrose, glycerol, or the like, and combinations thereof. In addition, if desired, the compositions may contain minor amounts of auxiliary substances such as wetting or emulsifying agents, stabilizing or pH buffering agents, and the like.

The compositions are conventionally administered parenterally, by injection, for example, either subcutaneously or intravenously. Additional formulations which are suitable for other modes of administration include suppositories, intranasal aerosols, and, in some cases, oral formulations. For suppositories, traditional binders and excipients may include, for example, polyalkylene glycols or triglycerides: such suppositories may be formed from mixtures containing the active ingredient in the range of 0.5% to 10%, preferably 1%-2%. Oral formulations include such normally employed excipients as, for example, pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharin, cellulose, magnesium carbonate, and the like. These compositions take the form of solutions, suspensions, tablets, pills, capsules, sustained release formulations, or powders, and contain 10%-95% of active ingredient, preferably 25%-70%. These oral formulations include formulations designed to protect the peptide until it can be absorbed.

The peptide compounds may be formulated into the compositions as neutral or salt forms. Pharmaceutically acceptable non-toxic salts include the acid addition salts (formed with the free amino groups) and which are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric, mandelic, and the like. Salts formed with the free carboxyl groups may be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, 2-ethylamino ethanol, histidine, procaine, and the like.

In addition to the compounds of the present invention which display thrombospondin-like activity, compounds of the present invention can also be employed as intermediates in the synthesis of such useful compounds.

The compounds of the invention can be homopolymerized to themselves (i.e., (peptide)_n) or, heteropolymerized to one another (i.e., (peptide 1-peptide 2). The compounds can also be cyclized through disulfide or other means. The compounds can also be conjugated to biocompatible polymeric compounds, such as BIOPOL™ (W. R. Grace & Co.-Conn.)

While not wishing to be bound by any theory, it is believed that the compositions of the invention act as agonists or antagonists to native thrombospondin. These compounds are also believed to act as agonists or antagonists to circumsporozoite protein, thrombospondin related anonymous protein, and properdin complement protein. Further, since the compounds of the invention are small in size (relative to intact thrombospondin) the properties which they exhibit are more likely to be specific in nature, as opposed to the actions of other generally adhesive compounds such as RGD containing compounds (the sequence of which is found in over a hundred proteins) and fibronectin. The side effects of the peptide compounds of the invention are greatly reduced when compared with these broadly adhesive compounds.

D. Use

As stated previously, the compounds of the invention can be used in a variety of biological, prophylactic or therapeutic areas. It is contemplated that these compounds are useful in prevention or treatment of any disease state or conditions wherein thrombospondin-like activity plays a role. These disease states and conditions include, but are not limited to, metastasis, wound healing, atherosclerosis, malaria, thrombotic conditions, thrombolytic conditions, angiogenesis, cell proliferation, and complement activation. Antibodies directed against the compounds of the invention are also useful as diagnostic reagents, therapeutics, or carriers of other compounds.

Numerous in vitro and in vivo assays can be used to demonstrate compounds having thrombospondin-like activity. These assays include, but are not limited to, cell adhesion assays, platelet aggregation assays and cell proliferation assays.

METASTASIS

Metastasis is the spread of disease from one part of the body to another unrelated to it, as in the transfer of the cells of a malignant tumor by way of the bloodstream or lymphatics. It is believed that metastasis is effected through a cascade mechanism which includes adhesion of tumor cells to endothelium, retraction of the endothelium, matrix degradation of the basement membrane and invasion of the tumor cells into the bloodstream. Intervention at any phase in this cascade could be beneficial to the treatment or prevention of metastatic cancers.

The native thrombospondin molecule has been shown to potentiate tumor cell metastasis (Tuszynski et al., Cancer Research (1987) 47:4130-4133). The mechanisms by which the thrombospondin potentiation occurs are not presently well understood.

Antimetastasis activity is characterized by the ability of the compounds to bind to melanoma cells in vitro (Tuszynski et al., Anal. Bio. (1990) 184:189-91), and the ability to reduce the size and number of tumor colonies in vivo (Tuszynski et al. Cancer Research (1987) 47:4130-4133).

The compounds of this invention are useful as antimetastatic agents, particularly useful as anti-pulmonary metastatic agents. These compounds inhibit the adhesion of metastatic tumor cells, particularly those which are responsive to thrombospondin. The compounds also reduce tumor colony number as well as tumor colony size.

There are a number of mechanisms by which such antimetastatic activity can be occurring. The peptides can be cytotoxic, or inhibit cell proliferation. As inhibitors of cell proliferation, the compounds can act to 1) inhibit mitogenesis, 2) inhibit angiogenesis, or 3) activate the complement pathway and the associated killer cells.

The compounds of the invention can also find use in biomedical devices. Since the compounds have the ability to promote the attachment of metastatic tumor cells, it is possible to coat a biomedical device with the compounds to effect the removal of circulating tumor cells from blood or lymph. The biomedical device is also useful to trap hepatomas.

Another use of the compounds is as a carrier to target toxins, drugs, hormones or imaging agents to metastatic tumor cells for diagnostic or therapeutic purposes. These carriers would also bind to hepatomas.

WOUND HEALING

Wound healing is the closure of wounds and can be divided into four essential components: inflammation, angiogenesis, collagen deposition and epithelialization. All four components play a role in the healing of wounds.

Wound healing activity is characterized by the ability of the compounds to show angiogenic activity, the ability of the compounds to stimulate collagen deposition and DNA synthesis in the in vivo sponge model or the ability of the compounds to improve wound healing or reduce healing time in an in vivo partial or full thickness wound model.

ATHEROSCLEROSIS

Atherosclerosis is a disease state which is characterized by the deposition of small fatty nodules on the inner walls of the arteries, often accompanied by degeneration of the affected areas.

Atherosclerosis activity is characterized by the capacity of the compounds to inhibit the development of aortic lesions in rabbits fed a high cholesterol diet.

MALARIA

Malaria is an infectious disease caused by any of various protozoans (genus Plasmodium) that are parasitic in the red blood corpuscles and are transmitted to mammals by the bite of an infected mosquito. The compounds of the invention can be used as antimalarial vaccines or as therapeutic agents to block cytoadherence.

Antimalarial activity is characterized by the ability to inhibit either the cytoadherence of malarial-infected red blood cells to endothelial cells, the malarial sporozoite recognition and entry into hepatocytes, or the malarial merozoite recognition and entry into red blood cells.

THROMBOTIC CONDITIONS

The thrombotic activity associated with the compounds of the invention acts to inhibit platelet aggregation and platelet thrombus formation. Platelets participate in blood coagulation via binding fibrinogen, platelet aggregation and thrombus formation. As anti-thrombotics, these peptides can be useful in the following conditions: myocardial infarction, thromboembolic disease and thrombotic complications due to cancer and cardiovascular disease.

The compounds of this invention have the ability to specifically inhibit the second stage of platelet aggregation (i.e., the thrombospondin dependent stage of platelet aggregation). This activity allows the compounds to be useful in inhibiting thrombocytopenia caused as a result of disease state (e.g., Acquired Immune Deficiency Syndrome (AIDS), Gray Platelet Syndrome, Essential Thrombocythemia, and Myeloproliferative Syndrome), or that may be induced by therapy (e.g., cancer therapy) or autoimmune diseases. For example, in Thrombotic Thrombocytopenia Purpura (TTP), generally associated with HIV cases, platelets are activated and consumed while producing high serum levels of platelet products. This results in a reduction of platelets in the blood and widespread hemorrhaging. Attentuating platelet activation (i.e., inhibiting platelet aggregation) will effectively inhibit TTP.

The compounds of this invention are useful in inhibiting thrombotic activity, and specifically inhibiting platelet aggregation activity. The use of the compounds of the present invention are also thereby useful in inhibiting TTP and thrombocytopenia. These compounds are further useful in preventing coronary artery reocculusion following balloon catheterization.

The compounds of this invention modulate the formation and structure of blood clots. Thrombospondin is incorporated into fibrin clots and serves as a substrate for blood clotting Factor XIIIa. An IQQ sequence motif in thrombospondin has been implicated in crosslinking to factor XIIIa. Peptides containing IQQ modulate structure and formation of clots. Known fibrinolytic in vitro assays demonstrate this ability.

Antithrombotic activity is characterized by a number of assays, including 1) inhibition of ADP or thrombin-induced platelet aggregation in washed platelets; 2) inhibition of platelet aggregation in platelet-rich plasma; 3) inhibition of collagen induced platelet aggregation measured in vivo; and 4) inhibition of induced thrombus formation in a carotid artery--in this assay the peptide would delay or prevent occlusion of the artery following thrombus induction.

Alternatively, the compounds of the present invention are useful as potent clotting agents. The effect can be localized and is long lasting. This activity is useful when clotting is necessary (i.e., surgery or in hemophilia).

THROMBOLYTIC CONDITIONS

The thrombolytic activity associated with the compounds of the invention act to alter the structure of a formed thrombus, i.e., dissolution of a blood clot. Thrombolytic activity is characterized as the ability to enhance the dissolution of fibrin in the presence of plasmin (i.e., standard clot lysis assay).

ANGIOGENESIS

Angiogenesis is the formation of blood and lymph vessels. The compounds of this invention are useful in the modulation of angiogenesis, particularly in enhancing wound healing, inhibiting or preventing tumor growth, diabetic retinopathy, and rheumatoid arthritis. Standard angiogenesis assays are well known in the art.

COMPLEMENT ACTIVITY

The complement activity associated with the compounds of the invention can play a role in a variety of disease states. The peptides enhance complement-mediated clearance and inactivation mechanisms in both natural and acquired resistance to infection. The complement activity of the peptides serves to promote tumoricidal activity of the complement protein C3b. Additionally, complement proteins are known to contribute to reperfusion injury following heart attacks, and the compounds of the invention can inhibit such activity and are thus useful to lessen heart tissue death and tissue injury during a heart attack.

ANTIVIRAL

Viral infections involve attachment to cells of viral particles. The peptides of this invention interfere with viral attachment and are thus useful as antiviral agents.

ANTIBODIES

Compounds of the present invention can also be used for perparing antisera for use in immunoassays employing labelled reagents, usually antibodies. Conveniently, the polypeptides can be conjugated to an antigen by means of dialdehydes, particularly from 4 to 6 carbon atoms and aliphatic, or carbodimide. These compounds and immunologic reagents may be labelled with a variety of labels such as chromophores, fluorophores such as, e.g., fluorescein or rhodamine, radioisotopes such as ¹²⁵ l, ³⁵ S, ¹⁴ C, or ³ H, or magnetized particles, by means well known in the art.

These labelled compounds and reagents, or labelled reagents capable of recognizing and specifically binding to them, can find use as, e.g., diagnostic reagents. Samples derived from biological specimens can be assayed for the presence or amount of substances having a common antigenic determinant with compounds of the present invention.

Thrombospondin levels are elevated in the serum of patients with metastatic breast and colon cancer (Tuszynski et al., Antithrombotic Therapy (1989) A28 and Smith et al., American Association of Clinical Oncology (in press)). Antibodies against the peptides of the invention can be useful as reagents in diagnostic/prognostic assays for various types of cancer, including but not limited to, gastrointestinal tract (gastric, colonic, and rectal) carcinomas, breast carcinomas and hepatic carcinomas.

In addition, monoclonal antibodies can be prepared by methods known in the art. The polyclonal and monoclonal antibodies can find therapeutic use in a number of cancer therapies. First, the antibodies can be used to sequester thrombospondin. This is useful since thrombospondin mediates tumor cell metastasis. Second, the antibodies can be used to block thrombospondin present on the tumor cell surface. Third, cytotoxic drugs, hormones, or imaging agents can be coupled to the antibodies for use in cancer therapy. Fourth, a biomedical device can be coated with the antibodies to remove excess thrombospondin from serum or to remove cells which bear thrombospondin on the cell surface.

The peptides of the invention can also be used to isolate thrombospondin cell surface receptors from extracts of cells or cell membranes. The thrombospondin cell surface receptors can be used to develop better thrombospondin analogs or to remove excess thrombospondin from serum.

ADHESION AND CELL ATTACHMENT

The peptides of the present invention can be used for preparing a surface for optimal cell culture, and for prosthetic materials to promote bonding with surrounding tissue. These peptides can be useful as a cell attachment protein to provide a substrate to which cells will attach by treating a hydrophobic surface such as untreated synthetic plastic resin and especially materials which are used for different membrane applications, e.g., nitrocellulose or polysulfone or comparable material with the peptide. The cell attachment properties of the peptides can also be used to couple polypeptides covalently to a solid support such as gels or synthetic resins or long chain polysaccharide. This latter approach can be used for different affinity chromatography applications. Another important application of using such peptides are the use of the peptide in commercial cell attachment surface, wherein the particles are coated with gelatin, making it possible to grow the same adherent cells in a much smaller volume of media than would be possible in dishes. Medical devices can be designed for use with such peptides to attach cells to the surface in vivo, or even to promote the growth of a desired cell type on particular surfaces prior to grafting. An example of this is attachment of islet cells to a membrane or growth of endothelial cells on a prosthetic blood vessel or vascular graft. Such peptides can find uses in coating a patch graft or the like for aiding in wound healing.

As herein described, cell adhesion activity is defined as the ability to promote or inhibit the attachment of cells to a substrate. It is believed that this dual function is achieved because the peptides of the present invention bind to the cells, and occupy all of the binding sites available on the cells. Therefore, when used for substrates, the peptides of the present invention find use to promote adhesion to substrates. The peptides of the present invention are also useful in effectively inhibiting cell-to-cell adhesion because the peptides occupy all of the available binding sites on the cells, thereby blocking these cells from binding to one another.

For example, endothelial cells resident on a vessel wall may be considered as constituting a substrate to which sickled red blood cells adhere resulting in vaso-occlusive crisis in sickle cell disease. Compounds which bind to both the endothelial cells and the sickled red blood cells can serve to block this adherence.

Sickle cell disease may, accordingly, be treated with compounds of the present invention due to their ability to essentially inhibit cell adhesion/aggregation. This is supported by recent studies. Hebble has shown that the adherence of sickle erythrocytes to human endothelial cells in vitro correlated directly with the clinical severity of vaso-occlusive morbidity in individual patients (BMJ, vol. 302(Jun. 29, 1991): p. 1551). In addition, further studies directed to thrombospondin have shown that thrombospondin, and peptides of thrombospondin are effective in inhibiting cell adhesion, and may have therapeutic use in sickle cell disease (Blood, vol. 80, No. 10 (November 1992): pp. 2634-2642).

Therefore, compounds such as those of the present invention, which inhibit the adherence of cells, would be useful in treating the sickle cell disease state, as well as other disease states that operate by cell adhesion.

The following examples are provided by way of illustration, rather than implying any limitation of the subject matter.

EXAMPLES

The peptides of this invention can be synthesized by conventional methods of peptide synthesis. A preferred method is the solid phase synthesis of Merrified, J. Amer. Chem. Soc. 85, 2149-2154 (1963); Science 150, 178-185 (1965); Ibid. 232, 341-347 (1986). Solid phase synthesis is generally initiated from the C-terminal of the peptide by coupling a protected alpha amino acid to a suitable resin, e.g., phenylacetamidomethyl (PAM) polystyrene resin, or p-methylbenzhydrylamine (mBHA) resin when synthesizing a peptide with a C-terminal carboxyamide. In the present invention, the peptides were synthesized by solid-phase techniques performed on an Applied Biosystems 430A Peptide Synthesizer (Foster City, Calif.) using t-butyloxycarbonyl (t-Boc) alpha amino-group protected amino acids in accordance with the instructions of the manufacturer. During this synthesis, suitable amino acid side-chain protecting groups are used as needed. Thus, aspartic acid is protected on the beta-carboxyl group as the benzyl ester and arginine is protected on the guanidino group by tosyl. After the desired peptide has been synthesized, the peptide is cleaved from the resin and protecting groups are removed by treatment with a reagent such as hydrogen fluoride (HF). The peptide can then be purified by high performance liquid chromatography (HPLC) or other such methods of peptide purification. Background information on the established procedures for solid phase peptide synthesis can be found in "Solid Phase Peptide Synthesis" by Stewart and Young, W. H. Freeman & Co., San Francisco, 1969.

In accordance with the above description, the following procedures were used for the chemical synthesis of novel synthetic peptides:

Procedure A

0.1 mmole of selected Boc-AA_n -OCH₂ -PAM Resin (0.2-0.8 mmole/g resin) (Applied Biosystems, Inc.) or p-mBHA Resin (0.2-0.7 mmole/g resin) (Applied Biosystems, Inc.) is treated according to Schedule A for the incorporation of the Boc-AA_n-1 or Boc-AA_n' respectively.

Schedule A. Small-scale Rapid Cycle Chemistry

1. 5-minute neat TFA wash

2. 40s DMF flow wash

3. 1-minute treatment with 20% DIEA in DMF

4. 40s DMF flow wash

5. Addition of 1-10 equivalents of preformed symmetric anhydride of a suitable protected t-boc amino acid dissolved in DMF

6. 10-minute coupling period

7. 40s DMF flow wash

Procedure B

0.5 mmole of selected Boc-AA_n -OCH₂ -PAM Resin (0.2-0.8 mmole/g resin) (Applied Biosystems, Inc.) or p-mBHA Resin (0.2-0.7 mmole/g resin) (Applied Biosystems.) is treated according to Schedule B for the incorporation of the Boc-AA_n-1 or BOC-AA_n' respectively.

Schedule B. Large-scale NMP/HOBT Chemistry

1. 3-minute wash with 30% TFA in DCM.

2. 17-minute wash with 50% TFA in DCM.

3. Wash 5× with DCM.

4. 1-minute wash with 5% DIEA in DCM.

5. 1-minute wash with 5% DIEA in NMP.

6. Wash 5× with NMP.

7. Addition of 1-4 equivalents of HOBT-ester of a suitably protected t-boc amino acid dissolved in NMP.

8. 30-minute coupling period.

9. Addition of DMSO to 20% and subsequent 16-minute coupling period.

10. Addition of 3.8 equivalents DIEA and subsequent 7-minute coupling period.

11. Wash 3× with DCM.

12. Wash with 10% acetic anhydride, 5% DIEA in DCM for 2 minutes.

13. Wash with 10% acetic anhydride in DCM for 4 minutes.

14. Wash 4× with DCM.

Example 1 Chemical Synthesis of WSPCSVTCG Compound p1

Briefly, 0.13 grams of t-boc-Gly-OCH₂ PAM resin (0.79 mmol/g) was subjected to the following sequential addition of suitably protected amino acids: t-boc-Cys(4-CH₃ Bzl), t-boc-Thr(Bzl), t-boc-Val, t-boc-Ser(Bzl), t-boc-Cys(4-CH₃ Bzl), t-boc-Pro, t-boc-Ser(Bzl), and t-boc-Trp. Resultant, dry, N-terminal protected peptidyl-resin was suspended in anhydrous hydrogen fluoride containing 5% anisole, 5% dimethyl sulfide, and 1% p-thiocresol for two hours at -5° C. HF and volatile scavengers were removed with nitrogen sparge and the peptide-resin mixture was suspended in cold diethyl ether. The peptide-resin mixture was washed three times with diethyl ether, then the peptide was extracted with 30% acetic acid. This solution was diluted 1:1 with H₂ O and lyophilized to afford the crude peptide. Purification was achieved on an Amicon C₁₈ MC-250-10 column utilizing reverse phase chromatography employing 0.1% aqueous trifluoroacetic acid with gradient generation afforded by the addition of 0.1% TFA in 90% acetonitrile and 10% H₂ O. Fractions were collected and pooled based on a purity of 90%, as judged by analytical reverse-phase HPLC. Pooled fractions were diluted with deoxygenated H₂ O and lyophilized to afford the pure peptide as a trifluoroacetic acid salt.

Example 2 Chemical Synthesis of WSPCSVTCG_NH.sbsb.2 SEQ ID NO:14! Compound p6

Briefly, 0.17 g of p-methylbenzyhydrylamine resin (0.62 mmol/g) was subjected to the following sequential addition of suitably protected amino acids: t-boc-Gly, t-boc-Cys(4-CH₃ Bzl), t-boc-Thr(Bzl), t-boc-Val, t-boc-Ser(Bzl), t-boc-Cys(4-CH₃ Bzl), t-boc-Pro, t-boc-Ser(Bzl), t-boc-Trp(CHO). The resultant n-terminal deprotected, formylated peptidyl-resin was dried then suspended is anhydrous HF containing 8% anisole and 2% dimethyl sulfide. Treatment was for 0.5 hours at -20° C. and 2 hours at 0° C. The HF was removed with nitrogen sparge. The peptide-resin mixture was suspended in and washed 3 times with diethyl ether. The peptide was extracted with 25% acetic acid. The resin was washed with 50% acetic acid and with H₂ O. The aqueous solutions were pooled, diluted 1:1 with deoxygenated H₂ O and lyophilized to afford the formylated crude peptide. Deformylation was effected using the procedure described in Applied Biosystems 430A User Bulletin 18. (Apr. 28, 1987). The peptide (5 mg/ml concentrate) in 6M guanidine-HCl was cooled to 0° C. and ethanolamine added to 1M. The pH is lowered to 6 with concentrated hydrochloric acid.

Purification was on an Amicon C₁₈ MC-250-10 column using reserve-phase chromatography. The ratio of acetonitrile to H₂ O was increased maintaining 0.1% TFA to achieve gradient elution. Collected fractions with a purity of 90%, as determined by analytical reverse-phase PHLC, were pooled, diluted with deoxygenated H₂ O and lyophilized to afford pure peptide as a trifluoroacetic acid salt.

Example 3 Chemical Synthesis of fWSPCSVTCG_NH.sbsb.2 SEQ ID NO:13! Compound p5

Briefly, procedure was same as for Example 2 except the deformylation step is not performed. The afforded crude peptide obtained past HF cleavage and subsequent lyophilization was purified as the formylated, C-terminal amide species.

Example 4 Other Thrombospondin Fragments or Analogs

Following the procedures outlined in Examples 1, 2 and 3 with appropriate modification, the following thrombospondin fragments or analogs were synthesized:

__________________________________________________________________________
CompoundStructure                                                         
__________________________________________________________________________
p18WDICSVTCG  SEQ ID NO:2!                                                
p19WSSCSVTCG  SEQ ID NO:3!                                                
p20WTSCSTSCG  SEQ ID NO:4!                                                
p11WSPWSEWTSCSTSCGNGIQQRGR  SEQ ID NO:5!                                  
p17WSHWSPWSSCSVTCGDGVITRIR  SEQ ID NO:6!                                  
p12WGPWSPWDICSVTCGGGVQKRSR  SEQ ID NO:7!                                  
WSPCSVTCS  SEQ ID NO:8!                                                   
WSQCSVTCG  SEQ ID NO:9!                                                   
WSQCNVTCG  SEQ ID NO:10!                                                  
WTPCSVTCG  SEQ ID NO:11!                                                  
p4DGGWSHWSPWSSCSVTCGDGVITR                                                
IRLCNSPSPQMNGKPCEGEARETKA                                                 
CKKDACPINGG  SEQ ID NO:12!                                                
__________________________________________________________________________

Example 5 Direct Adhesion Assay

It is believed that thrombospondin acts in metastasis through its adhesive properties. An assay was developed, generally in accordance with the disclosure of Tuszynski et al. (Anal. Bio. (1990) 184:189-91) which evaluates the ability of melanoma cells to adhere to the thrombospondin fragments or analogs of the invention. In this assay, wells of a 96-well microtiter dish (Costar, Cambridge, Mass.) were incubated for two to three hours with 50 μl of a 40 μg/ml solution of various ligands in 20 mM NaCl, pH 7.3. Thrombospondin (purified by the method of Tuszynski et al., J. Biol. Chem. (1985) 260:12240-5), fibronectin (Sigma Chemical Co., Missouri) served as the positive control. Bovine serum albumin (BSA) (Sigma Chemical Co.) served as the negative control. Thrombospondin analogs of the invention p1, p5 and p6 were synthesized as described in Examples 1 through 3. Following peptide adhesion to the microtiter dish, the wells were aspirated, treated with 200 μl phosphate buffered saline (PBS) containing 1% BSA for 1 hour and then washed three more times with 200 μl PBS.

Mouse B₁₆ F₁₀ melanoma cells were grown and harvested during log phase of growth using standard procedures. The harvested cells were washed two times in serum-free Dulbecco's minimum essential medium (DMEM) (Flow Laboratories) and suspended in DMEM at a final concentration of 4×10⁵ cells/ml. Of the cell suspension 100 μl was added to each well of the microtiter dish containing the various ligands and the dish incubated at 37° C. in a CO₂ incubator for 1 hour. Nonadherent cells were removed by aspiration and the wells washed three times with 200 μl of PBS. The total cell-associated protein was determined by dissolving the attached cells directly in the microtiter wells with 200 μl of the Pierce BCA working solution (Pierce Chem. Co. Booklet No. 23225 (1987)). The plate was covered with an adhesive mylar sheet (Flow Labs) and incubated at 60° C. for 30 minutes. Plates were allowed to cool to room temperature, cover sheets were removed, and the absorbance of each well was determined at 562 nm with a microtiter plate reader (Biotek, Burlington, Vt.)

The results shown in Table 1 indicate that the peptides of the inventions p1, p5, and p6 display adhesive properties.

              TABLE 1                                                     
______________________________________                                    
Absorbed                                                                  
Compound (2 μg)                                                        
             Adhesion as % Thrombospondin                                 
______________________________________                                    
Thrombospondin                                                            
             100                                                          
pl           98                                                           
p5           79                                                           
p6           70                                                           
BSA          13                                                           
______________________________________

Example 6 Competitive Assay to Measure Thrombospondin Specific Adhesion to Melanoma Cells

The direct adhesion assay of Example 5 was modified to measure the ability of the peptide compounds of the invention to compete with intact thrombospondin for adhesion to melanoma cells.

In this assay, intact thrombospondin is absorbed onto microtiter dishes as described in Example 5. The assay is similar to Example 5 except that before the melanoma cells are added to the microtiter dishes they are preincubated for 15 minutes with 100 μg/ml of various ligands.

The results shown in Table 2 indicate that peptide p1 is able to effectively compete with thrombospondin for adhesion to melanoma cells. Peptides p5 and p6 compete to a lesser degree at this concentration.

              TABLE 2                                                     
______________________________________                                    
             Concentration                                                
Compound     (μg/ml) % of buffer control                               
______________________________________                                    
buffer       --         100                                               
pl           100        20                                                
             100        42                                                
             50         40                                                
             10         49                                                
p5           100        62                                                
             100        108                                               
             50         104                                               
             10         99                                                
             100        83                                                
             200        89                                                
             300        83                                                
p6           100        89                                                
             200        74                                                
             300        74                                                
______________________________________

Example 7 Direct Platelet Adhesion Assay

The number of adherent platelets was essentially determined as previously described (Tuszynski et al., Anal. Bio. supra). Briefly, 100 μl of 5×10⁸ platelets/ml washed as previously described (Tuszynski, et al., Blood 72, 109-225, 1988) were added to microtiter plates, the wells of which were treated with 50 μl of a 40 μg/ml peptide or protein solution (Hepes buffered saline, pH 7.4). Solutions were dried at room temperature after incubation in a fume hood for two hours. Wells were blocked for one hour with 1% BSA. Platelets (100 μl) were incubated in the wells for 30 minutes and non-adherent platelets were removed by aspiration. Wells were washed 3× with 200 μl of Hepes buffered saline, pH 7.4. The number of adherent platelets was determined by measuring the platelet-derived protein using the BCA protein assay.

The results shown in Table 3 indicate that at this concentration p1, p6, and to a lesser degree, p5 adhere to platelets.

              TABLE 3                                                     
______________________________________                                    
Compound      Adherence as % Control                                      
______________________________________                                    
Thrombospondin                                                            
              100                                                         
BSA           0.7                                                         
p1            39                                                          
p5            2.1                                                         
p6            38                                                          
fibronectin   83                                                          
______________________________________

Example 8 Competitive Assay to Measure Thrombospondin Specific Adhesion to Platelets

The direct adhesion assay of Example 7 was modified to measure the ability of the peptide compounds of the invention to compete with intact thrombospindin or fibronectin for adhesion of platelets.

In this assay, thrombospondin (TSP) or fibronectin (FN) was absorbed onto microtiter dish as described in Example 7. The assay was similar to Example 7 except that before platelets were added to the microtiter dishes they were preincubated with 250 μg/ml of various ligands.

The results shown in Table 4 indicate that peptide p1 effectively competed with thrombospondin for platelet adhesion, but did not compete with fibronectin.

              TABLE 4                                                     
______________________________________                                    
          Concentration Absorbed % Buffer                                 
Compound  (μg/ml)    Protein  Control                                  
______________________________________                                    
buffer    --            TSP      100                                      
p1        250           TSP      71                                       
p5        250           TSP      107                                      
p6        250           TSP      98                                       
buffer    --            FN       100                                      
p1        250           FN       108                                      
p5        250           FN       109                                      
p6        250           FN       96                                       
______________________________________

Example 9 Platelet Aggregation Assay

Platelet aggregation was monitored on a single-channel aggregometer equipped to measure luminescence (Chromo-Log, Havertown, Pa.). Platelet-rich-plasma (PRP) was obtained from whole blood anti-coagulated with 0.38% Sodium Citrate by centrifugation at 150×g for 20 minutes. Peptides were added to 0.5 ml of PRP and aggregation initiated with 1 μM ADP. Buffer blanks contained diluent (water) but no peptide.

The results shown in FIG. 1 indicate that p1, p5 and p6 inhibit platelet aggregation.

Example 10 Antimetastatic Activity In Vivo

The in vivo model used to demonstrate the antimetastatic activity of the peptide compounds of the invention is described by Tuszynski et al. (Cancer Res. (1987) 47:4130-4133). Briefly, C57 black mice were intravenously injected with 5×10⁵ B₁₆ F₁₀ mouse melanoma cells in the presence of either control buffer (Hepes buffered saline, pH 7.4), or the indicated amount of peptide compound of the invention p1, p5 or p6. After 16 days, the mice were sacrificed and the number of lung tumors counted.

The results shown in Table 5 indicate the peptides of the invention have antimetastatic activity. The p1-, p5- and p6-treated animals developed statistically fewer tumors than controls. Additionally, the lung tumors were smaller in size in the p1- and p6-treated animals.

              TABLE 5                                                     
______________________________________                                    
             Concentration                                                
Compound     μg/mouse                                                  
                        % buffer control                                  
______________________________________                                    
buffer       --         100                                               
pl           30         49                                                
p5           30         87                                                
p6           30         91                                                
p6           100        102                                               
p6           300        50                                                
______________________________________

__________________________________________________________________________
SEQUENCE LISTING                                                          
(1) GENERAL INFORMATION:                                                  
(iii) NUMBER OF SEQUENCES: 15                                             
(2) INFORMATION FOR SEQ ID NO:1:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:                                   
TrpSerProCysSerValThrCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:2:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:                                   
TrpAspIleCysSerValThrCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:3:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:                                   
TrpSerSerCysSerValThrCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:4:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:                                   
TrpThrSerCysSerThrSerCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:5:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 23 amino acids                                                
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:                                   
TrpSerProTrpSerGluTrpThrSerCysSerThrSerCysGlyAsn                          
151015                                                                    
GlyIleGlnGlnArgGlyArg                                                     
20                                                                        
(2) INFORMATION FOR SEQ ID NO:6:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 23 amino acids                                                
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:                                   
TrpSerHisTrpSerProTrpSerSerCysSerValThrCysGlyAsp                          
151015                                                                    
GlyValIleThrArgIleArg                                                     
20                                                                        
(2) INFORMATION FOR SEQ ID NO:7:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 23 amino acids                                                
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:                                   
TrpGlyProTrpSerProTrpAspIleCysSerValThrCysGlyGly                          
151015                                                                    
GlyValGlnLysArgSerArg                                                     
20                                                                        
(2) INFORMATION FOR SEQ ID NO:8:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:                                   
TrpSerProCysSerValThrCysSer                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:9:                                          
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:                                   
TrpSerGlnCysSerValThrCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:10:                                         
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:10:                                  
TrpSerGlnCysAsnValThrCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:11:                                         
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:11:                                  
TrpThrProCysSerValThrCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:12:                                         
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 60 amino acids                                                
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:                                  
AspGlyGlyTrpSerHisTrpSerProTrpSerSerCysSerValThr                          
151015                                                                    
CysGlyAspGlyValIleThrArgIleArgLeuCysAsnSerProSer                          
202530                                                                    
ProGlnMetAsnGlyLysProCysGluGlyGluAlaArgGluThrLys                          
354045                                                                    
AlaCysLysLysAspAlaCysProIleAsnGlyGly                                      
505560                                                                    
(2) INFORMATION FOR SEQ ID NO:13:                                         
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(ix) FEATURE:                                                             
(A) NAME/KEY: Peptide                                                     
(B) LOCATION: 1                                                           
(D) OTHER INFORMATION: the tryptophan at position                         
1 is n- formyl-tryptophan."                                               
(ix) FEATURE:                                                             
(A) NAME/KEY: Peptide                                                     
(B) LOCATION: 9                                                           
(D) OTHER INFORMATION: the glycine at position 9                          
is carboxyamide."                                                         
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:13:                                  
TrpSerProCysSerValThrCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:14:                                         
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(ix) FEATURE:                                                             
(A) NAME/KEY: Peptide                                                     
(B) LOCATION: 9                                                           
(D) OTHER INFORMATION: the glycine at position 9                          
is carboxyamide glycine."                                                 
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:14:                                  
TrpSerProCysSerValThrCysGly                                               
15                                                                        
(2) INFORMATION FOR SEQ ID NO:15:                                         
(i) SEQUENCE CHARACTERISTICS:                                             
(A) LENGTH: 9 amino acids                                                 
(B) TYPE: amino acid                                                      
(C) STRANDEDNESS:                                                         
(D) TOPOLOGY: linear                                                      
(ii) MOLECULE TYPE: peptide                                               
(xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:                                  
XaaXaaXaaCysXaaXaaXaaCysXaa                                               
15                                                                        
__________________________________________________________________________

Claims

What is claimed is:

1. A method for mimicking a biological activity of thrombospondin, the method comprising administering an effective amount of a polypeptide compound having the formula:

Z.sub.1 -AA.sub.1 -AA.sub.2 -AA.sub.3 -AA.sub.4 -AA.sub.5 -AA.sub.6 -AA.sub.7 -AA.sub.8 -AA.sub.9 -Z.sub.2                    (SEQ ID NO: 15)

wherein:

Z₁ is selected from the group consisting of hydrogen, amino, acetyl, at least one amino acid residue, and at least one desamino form of an amino acid residue;

AA₁ is a neutral/nonpolar/large/cyclic amino acid residue;

AA₂ is selected from the group consisting of a neutral/polar/small amino acid residue, a neutral/polar/large/non-cyclic amino acid residue, and an acidic amino acid residue;

AA₃ is selected from the group consisting of a neutral/non-polar/large/cyclic amino acid residue, a neutral/nonpolar/large/non-cyclic amino acid residue, a neutral/polar/large/non-cyclic amino acid residue, and a neutral/polar/small amino acid residue;

AA₄ is a neutral/polar/small amino acid residue;

AA₅ is selected from the group consisting of a neutral/polar/small amino acid residue and a neutral/polar/large/non-cyclic amino acid residue;

AA₆ is selected from the group consisting of a neutral/nonpolar/large/non-cyclic amino acid residue and a neutral/polar/large/non-cyclic amino acid residue;

AA₇ is selected from the group consisting of a neutral/polar/large/non-cyclic amino acid residue and a neutral/polar/small amino acid residue;

AA₈ is a neutral/polar/small amino acid residue;

AA₉ is a neutral/polar/small amino acid residue; and

Z₂ is selected from the group consisting of hydroxyl, carboxyl, a non-amino acid, agmatine, at least one amino acid residue, at least one carboxyamide form of an amino acid residue, and at least one alkylamide form of an amino acid residue.

2. The method of claim 1 wherein:

AA₁ is selected from the group consisting of tryptophan and n-formyl-tryptophan;

AA₂ is selected from the group consisting of serine, threonine, and aspartic acid;

AA₃ is selected from the group consisting of proline, glutamic acid, serine, and isoleucine;

AA₄ is cysteine;

AA₅ is selected from the group consisting of serine and asparagine;

AA₆ is selected from the group consisting of valine and threonine;

AA₇ is selected from the group consisting of threonine and serine;

AA₈ is cysteine; and

AA₉ is selected from the group consisting of glycine, serine, the carboxyamide form of glycine, and the carboxyamide form of serine.

3. The method of claim 2 wherein the polypeptide compound has a sequence selected from the group consisting of:

W-S-P-C-S-V-T-C-G SEQ ID NO:1!,

fW-S-P-C-S-V-T-C-G-NH₂ SEQ ID NO:13!,

W-S-P-C-S-V-T-C-G-NH₂ SEQ ID NO:14!,

W-D-I-C-S-V-T-C-G SEQ ID NO:2!,

W-S-S-C-S-V-T-C-G SEQ ID NO:3!,

W-T-S-C-S-T-S-C-G SEQ ID NO:4!,

W-S-P-W-S-E-W-T-S-C-S-T-S-C-G-N-G-I-Q-Q-R-G-R SEQ ID NO:5!,

W-S-H-W-S-P-W-S-S-C-S-V-T-C-G-D-G-V-I-T-R-I-R SEQ ID NO:6!,

W-G-P-W-S-P-W-D-I-C-S-V-T-C-G-G-G-V-Q-K-R-S-R SEQ ID NO:7!,

W-S-P-C-S-V-T-C-S SEQ ID NO:8!,

W-S-Q-C-S-V-T-C-G SEQ ID NO:9!,

W-S-Q-C-N-V-T-C-G SEQ ID NO:10!,

W-T-P-C-S-V-T-C-G SEQ ID NO:11!, and

D-G-G-W-S-H-W-S-P-W-S-S-C-S-V-T-C-G-D-G-V-I-T-R-I-R-L-C-N-S-P-S-P-Q-M-N-G-K-P-C-E-G-E-A-R-E-T-K-A-C-K-K-D-A-C-P-I-N-G-G SEQ ID NO:12!

4. The method of claim 1 wherein the biological activity is platelet aggregation activity.

5. The method of claim 1 wherein the biological activity is antiviral activity.

6. The method of claim 1 wherein the biological activity is complement activation.

7. The method of claim 1 wherein the polypeptide compounds are homopolymerized or heteropolymerized, conjugated or cyclized.

8. The method of claim 1 wherein said polypeptide compound is admixed with at least one pharmaceutically acceptable carrier prior to being administered.

9. A composition for mimicking a biological activity of thrombospondin, the composition comprising a pharmaceutically acceptable carrier together with an effective amount of a polypeptide compound having the formula:

Z.sub.1 -AA.sub.1 -AA.sub.2 -AA.sub.3 -AA.sub.4 -AA.sub.5 -AA.sub.6 -AA.sub.7 -AA.sub.8 -AA.sub.9 -Z.sub.2                    (SEQ ID NO: 15)

wherein:

AA₁ is a neutral/nonpolar/large/cyclic amino acid residue;

AA₄ is a neutral/polar/small amino acid residue;

AA₈ is a neutral/polar/small amino acid residue;

AA₉ is a neutral/polar/small amino acid residue; and

10. A method for promoting thrombotic activity, the method comprising administering an effective amount of a polypeptide compound having the formula:

Z.sub.1 -AA.sub.1 -AA.sub.2 -AA.sub.3 -AA.sub.4 -AA.sub.5 -AA.sub.6 -AA.sub.7 -AA.sub.8 -AA.sub.9 -Z.sub.2                    (SEQ ID NO: 15)

wherein:

AA₁ is a neutral/nonpolar/large/cyclic amino acid residue;

AA₄ is a neutral/polar/small amino acid residue;

AA₈ is a neutral/polar/small amino acid residue;

AA₉ is a neutral/polar/small amino acid residue; and

11. The method of claim 10 wherein said polypeptide compound has a sequence selected from the group consisting of:

W-S-P-C-S-V-T-C-G SEQ ID NO:1!,

fW-S-P-C-S-V-T-C-G-NH₂ SEQ ID NO:13!,

W-S-P-C-S-V-T-C-G-NH₂ SEQ ID NO:14!,

W-D-I-C-S-V-T-C-G SEQ ID NO:21!,

W-S-S-C-S-V-T-C-G SEQ ID NO:3!,

W-T-S-C-S-T-S-C-G SEQ ID NO:4!,

W-S-P-W-S-E-W-T-S-C-S-T-S-C-G-N-G-I-Q-Q-R-G-R SEQ ID NO:5!,

W-S-H-W-S-P-W-S-S-C-S-V-T-C-G-D-G-V-I-T-R-I-R SEQ ID NO:6!,

W-G-P-W-S-P-W-D-I-C-S-V-T-C-G-G-G-V-Q-K-R-S-R SEQ ID NO:7!,

W-S-P-C-S-V-T-C-S SEQ ID NO:8!,

W-S-Q-C-S-V-T-C-G SEQ ID NO:9!,

W-S-Q-C-N-V-T-C-G SEQ ID NO:10!,

W-T-P-C-S-V-T-C-G SEQ ID NO:11!, and

12. The method of claim 10 wherein the thrombotic activity is clotting of blood.

13. A method for inhibiting a biological activity of thrombospondin, the method comprising administering an effective amount of a polypeptide compound having the formula:

Z.sub.1 -AA.sub.1 -AA.sub.2 -AA.sub.3 -AA.sub.4 -AA.sub.5 -AA.sub.6 -AA.sub.7 -AA.sub.8 -AA.sub.9 -Z.sub.2                    (SEQ ID NO: 15)

wherein:

AA₁ is a neutral/nonpolar/large/cyclic amino acid residue;

AA₄ is a neutral/polar/small amino acid residue;

AA₈ is a neutral/polar/small amino acid residue;

AA₉ is a neutral/polar/small amino acid residue;

Z₂ is selected from the group consisting of hydroxyl, carboxyl, a non-amino acid, agmatine, at least one amino acid residue, at least one carboxyamide form of an amino acid residue, and at least one alkylamide form of an amino acid residue; and

wherein said biological activity is not thrombotic activity.

14. The method of claim 13 wherein:

AA₄ is cysteine;

AA₅ is selected from the group consisting of serine and asparagine;

AA₆ is selected from the group consisting of valine and threonine;

AA₇ is selected from the group consisting of threonine and serine;

AA₈ is cysteine; and

15. A composition for inhibiting a biological activity of thrombospondin, the composition comprising a pharmaceutically acceptable carrier together with an effective amount of a polypeptide compound having the formula:

Z.sub.1 -AA.sub.1 -AA.sub.2 -AA.sub.3 -AA.sub.4 -AA.sub.5 -AA.sub.6 -AA.sub.7 -AA.sub.8 -AA.sub.9 -Z.sub.2                    (SEQ ID NO: 15)

wherein:

AA₁ is a neutral/nonpolar/large/cyclic amino acid residue;

AA₄ is a neutral/polar/small amino acid residue;

AA₈ is a neutral/polar/small amino acid residue;

AA₉ is a neutral/polar/small amino acid residue;

wherein said biological activity is not thrombotic activity.

16. The method of claim 10 wherein:

AA₄ is cysteine;

AA₅ is selected from the group consisting of serine and asparagine;

AA₆ is selected from the group consisting of valine and threonine;

AA₇ is selected from the group consisting of threonine and serine;

AA₈ is cysteine; and

17. The method of claim 1 wherein the biological activity is immune modulation.